The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127797501 12779750 1 I 20160921 20160926 20160926 PER US-PFIZER INC-2016444436 PFIZER 55.00 YR M Y 120.00000 KG 20160926 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127797501 12779750 1 PS REVATIO SILDENAFIL CITRATE 1 20 MG, 3X/DAY A563501 21845 20 MG FILM-COATED TABLET TID
127797501 12779750 2 SS REVATIO SILDENAFIL CITRATE 1 40 MG, 3X/DAY 21845 40 MG FILM-COATED TABLET TID
127797501 12779750 3 C TRACLEER BOSENTAN 1 125 MG, 2X/DAY 0 125 MG BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127797501 12779750 1 Pulmonary arterial hypertension
127797501 12779750 3 Pulmonary arterial hypertension

Outcome of event

Event ID CASEID OUTC COD
127797501 12779750 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127797501 12779750 Condition aggravated
127797501 12779750 Headache
127797501 12779750 Pre-existing condition improved
127797501 12779750 Product use issue
127797501 12779750 Pulmonary hypertension
127797501 12779750 Therapeutic response unexpected

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
127797501 12779750 1 2014 0
127797501 12779750 3 2007 0